Cited by 186Prostate Cancer Treatment and ResearchChemotherapy-induced cardiotoxicity and mitigationHormonal and reproductive studies

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Cardiovascular Side Effects of Diethylstilbestrol, Cyproterone Acetate, Medroxyprogesterone Acetate and Estramustine Phosphate Used for the Treatment of Advanced Prostatic Cancer: Results from European Organization for Research on Treatment of Cancer Trials 30761 and 30762

de Voogt, Herman J., Smith, Philip H., Pavone-Macaluso, Michele, de Pauw, Marleen, Suciu, Stefan, Members of the European Organization for Research on Treatment of Cancer Urological Group·1986·Journal of Urology

Abstract

Two randomized trials were started in 1976 by the European Organization for Research on Treatment of Cancer urological group. Trial 30761 compared 1 mg. diethylstilbestrol orally 3 times daily to 250 mg. oral cyproterone acetate daily and to 500 mg. medroxyprogesterone acetate intramuscularly 3 times weekly for 8 weeks, then 200 mg. orally daily. Trial 30762 compared 3 mg. diethylstilbestrol to 560 mg. estramustine phosphate orally for 8 weeks and then 280 mg. daily. The 239 patients in study 30761 and 226 in study 30762 were evaluated for cardiovascular toxicity during treatment. Various types of side effects (fluid retention, hypertension, electrocardiographic changes, myocardial infarction and thromboembolic disease) and their degrees of severity were analyzed. In both studies the most frequent type of cardiovascular toxicity was represented by fluid retention. Cardiovascular toxicity as a whole was higher with diethylstilbestrol than with estramustine phosphate or medroxyprogesterone acetate therapy, and was the lowest with cyproterone acetate therapy. The risk of severe cardiovascular complications developing was the highest during the first 6 months of treatment. Increasing age, body weight greater than 75 kg. and, especially, the presence of previous cardiovascular disease represented adverse factors in the development of cardiovascular toxicity.

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Crossref · 10.1016/s0022-5347(17)45620-5

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1 of 1 references verified0 citation errors · 0 not checkable

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  • All three agents (progestogens, antiandrogens, GnRH analogues) are associated with potential adverse effects such as precipitation or aggravation of cardiac conditions, gynaecomastia, weight gain, hot flushes, or depression.

    “All three agents are associated with potential adverse effects (Reilly 2000), such as precipitation or aggravation of cardiac conditions (De Voogt 1986; Pierce 1995), gynaecomastia, weight gain, hot flushes, or depression (Grubin 2008).”

Citations

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Research works printed but not linked: 11

  1. Pavone-Macaluso, 1980, EORTC protocols in prostatic cancer. An interim report, Scand. J. Urol. Nephrol., 55, 163
  2. Pavone-Macaluso, 1983, Medroxyprogesterone acetate in the treatment of prostatic cancer: preliminary results of EORTC trial 30761 comparing medroxyprogesterone acetate with stilbestrol and with cyproterone acetate, vol. 2, 183
  3. Sylvester, 1980, On the analysis of response rates in studies of advanced disease, Eur. J. Cancer, 16, 5
  4. Gehan, 1969, Estimating survival functions from the life table, J. Chron. Dis., 21, 629, 10.1016/0021-9681(69)90035-6 · DOI
  5. Smith, 1970, A computer program for estimating survival functions from the life table, Comput. Prog. Biomed., 1, 58, 10.1016/0010-468X(70)90014-0 · DOI
  6. 1967, The Veterans Administration Cooperative Urological Research Group: Carcinoma of the prostate: treatment comparisons, J. Urol., 98, 516, 10.1016/S0022-5347(17)62926-4 · DOI
  7. Byar, 1973, The Veterans Administration Cooperative Urological Research Group’s studies of cancer of the prostate, Cancer, 32, 1126, 10.1002/1097-0142(197311)32:5<1126::AID-CNCR2820320518>3.0.CO;2-C · DOI
  8. Byar, 1980, Review of the Veterans Administration studies of cancer of the prostate and new results concerning treatment of stage I and II tumors, 471
  9. Shearer, 1973, Plasma testosterone: an accurate monitor of hormone treatment in prostatic cancer, Brit. J. Urol., 45, 668, 10.1111/j.1464-410X.1973.tb12238.x · DOI
  10. Gordon, 1974, Differences in coronary heart disease in Framingham, Honolulu and Puerto Rico, J. Chron. Dis., 27, 329, 10.1016/0021-9681(74)90013-7 · DOI
  11. 1982, The Italian Research Group of the Seven Countries study: Incidence and prediction of coronary heart disease in two Italian rural population samples followed-up for 20 years, Acta Cardiol., 37, 129

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Metadata

Authors
de Voogt, H. J., Smith, P. H., Pavone-Macaluso, M., de Pauw, M., Suciu, S., & Members of the European Organization for Research on Treatment of Cancer Urological Group
Affiliations
  • St James's University Hospital (GB)
  • From the Free University, Amsterdam, The Netherlands
Venue
Journal of Urology
Published
1986-02
Volume
135
Issue
2
Pages
303-307
ISSN
  • 0022-5347 (ISSN-L)
  • 1527-3792
OpenAlex
W38359027
Cited by
186
References
1
Citations by year
2025: 1 · 2024: 1 · 2023: 1 · 2020: 4 · 2019: 1 · 2017: 4 · 2016: 1 · 2015: 4 · 2014: 3 · 2013: 4 · 2012: 7
FWCI
16.12
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Urology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Cancer Institute (5R10CA11488-11)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Prostate Cancer Treatment and Research
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Chemotherapy-induced cardiotoxicity and mitigation
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
Keywords
advanced prostate cancer, cardiotoxicity, diethylstilbestrol, cyproterone acetate, medroxyprogesterone acetate, estramustine phosphate, fluid retention, hypertension, electrocardiographic changes, myocardial infarction, thromboembolism, risk factors, androgen deprivation therapy
MeSH terms
Aged, Body Weight, Cardiovascular Diseases, Clinical Trials as Topic, Cyproterone, Diethylstilbestrol, Estramustine, Europe, Humans, Male, Medroxyprogesterone, Middle Aged, Nitrogen Mustard Compounds, Prostatic Neoplasms, Random Allocation, Time Factors, Medroxyprogesterone Acetate, Cyproterone Acetate

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